Table 1.
Tissue | Bioink | Cell Type | Strategy | Achievement | Ref. |
---|---|---|---|---|---|
Cartilage | Nanocellulose-alginate bioink | Human nasoseptal chondrocytes | Physical combination | Constructs with high fidelity and stability | [161] |
hyaluronic acid/alginate bioink, PCL as a scaffold | Human articular chondrocytes | Physical combination | Improved printability, gelling abilities, stiffness and degradability | [162] | |
Alginate Sulfate–Nanocellulose Bioinks | Bovine chondrocytes | Chemical modification | High shape fidelity, good printability | [163] | |
Nanocellulose/Alginate Bioink | iPSCs | Physical combination | Bioprinted iPSCs for cartilage regeneration | [164] | |
Collagen-alginate bioink | Rat chondrocytes | Physical combination | Improved mechanical strength, enhanced cells adhesion, proliferation | [87] | |
Polylactic Acid (PLA) Nanofiber−Alginate Hydrogel Bioink | Human adipose-derived stem cells | Physical combination | Improved hASC metabolic activity and proliferation | [165] | |
Alginate, gelatin, and fibrinogen as bioink | hMSCs | Physical combination | The addition of TGF-β1 and BMP-2 promoted cells differentiation | [166] | |
Alginate and short sub-micron polylactide (PLA) fibers | Human chondrocytes | Physical combination | High cell viability | [167] | |
Bone | alginate-sulfate bioink | MC3T3-E1 osteoblasts | Chemical modification | Improved osteoblastic proliferation and differentiation | [152] |
Graphene oxide/alginate bioink | hMSCs | Physical combination | Enhanced osteogenic differentiation, improved printability | [168] | |
Alginate CaCl2 bioink | Human bone marrow-derived MSCs | Chemical modification | Increased osteogenic differentiation | [169] | |
RGD-γ-irradiated alginate and nano-hydroxyapatite (nHA) complexed to plasmid DNA (pDNA) |
Human bone marrow-derived MSCs | Chemical modification | Superior levels of vascularization and mineralization | [170] | |
Vessel | Sodium alginate Fibroblasts |
L929 mouse fibroblasts | Collaborative 3D bioprinting | Multilevel fluidic channels | [171] |
Sodium alginate, collagen | HUVECs | Microgel-bioink-based 3D bioprinting | Achieved rapid and efficient in vivo angiogenesis. |
[172] | |
VdECM/alginate bioink | HUVEC/HAoSMCs | Collaborative 3D bioprinting | As transplants in vivo for three weeks | [160] | |
gelatin-based alginate/carbon nanotubes blend bioink | Fibroblasts | Physical combination | Enhanced mechanical properties | [173] | |
Gelatin-methacryloyl (GelMA) + PEGDA + alginate lyase | Vascular smooth muscle cells/vascular endothelial cells | Collaborative 3D bioprinting & Physical combination | Two-cell-layered structure | [174] | |
Skin | Gelatin and sodium alginate hydrogel, fibroblast cells | Fibroblasts | Physical combination | Situ 3D bioprinting | [175] |
Sodium alginate, sodium carboxymethyl cellulose | / | Physical combination | Repaired rabbit wound defeat | [176] | |
Nerve scaffold | Sodium alginate, gelatin | Rat Schwann cells | Physical combination | Improved cell adhesion and related factor expression, in vivo | [177] |
Muscle | Gelatin Methacryloyl-Alginate Bioinks |
Mouse C2C12 myoblast cells | Collaborative 3D bioprinting | Dually crosslinking can provide the optimal niche for muscle tissue formation | [178] |
PEG-Fibrinogen (PF)/alginate | Human C2C12 myoblast cells | Collaborative 3D bioprinting | Formed multinucleated myotubes | [179] |